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. 2025 Apr 30;17(9):1552.
doi: 10.3390/nu17091552.

Isolation, Characterization, and Anti-Allergic Evaluation of Phytochemicals from Wikstroemia trichotoma

Affiliations

Isolation, Characterization, and Anti-Allergic Evaluation of Phytochemicals from Wikstroemia trichotoma

Min-Ji Keem et al. Nutrients. .

Abstract

Background/Objectives: The Wikstroemia genus has been traditionally used in Asia to treat various ailments, including parotitis, pneumonia, and pertussis. These plants contain many bioactive compounds, including flavonoids, coumarins, and lignans. This study investigates the chemical components of a MeOH extract of the aerial parts of Wikstroemia trichotoma (Thunb.) Makino and evaluates their anti-inflammatory and anti-allergic effects in vitro. Methods: Chromatographic techniques, spectroscopic analysis, and the literature were used to isolate compounds from the branches and leaves of W. trichotoma. IL-4 mRNA and β-hexosaminidase levels were assessed by performing assays on RBL-2H3 cells to evaluate anti-inflammatory and anti-allergic potential. Results: Forty-two compounds were isolated from the W. trichotoma extract, and the flavanones trichotocinol A and B were newly identified. Screening of isolated compounds showed that several significantly inhibited DNP-BSA-induced β-hexosaminidase release by 10.0-58.0% and PMA/ionomycin-induced IL-4 mRNA expression by 25.3-71.7% versus negative controls. In addition, trichotocinol A reduced IL-4 mRNA expression by 31.9%. Conclusions: The discovery of these new compounds contributes to our understanding of the bioactive properties of W. trichotoma and suggests their potential use as natural therapeutic agents for inflammatory disorders.

Keywords: Wikstroemia trichotoma; anti-allergy; anti-inflammation; flavonoid; interleukin 4; β-hexosaminidase.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Chemical structures of the isolated compounds (142) from the W. trichotoma extract.
Figure 2
Figure 2
Selected COSY (formula image) and HMBC (→) correlations of compounds 1 and 2.
Figure 3
Figure 3
Inhibitory effects of the compounds isolated from the MeOH extract of W. trichotoma on PMA/ionomycin-induced IL-4 mRNA expression in RBL-2H3 cells. Data are presented as means ± SDs (n = 2), and significance was accepted for ### p value < 0.001 versus non-treated cells, and * p < 0.05, ** p < 0.01, *** p < 0.001 versus PMA/ionomycin-treated cells. PMA, phorbol 12-myristate 13-acetate; CsA, cyclosporin A; IL-4, interleukin-4.
Figure 4
Figure 4
Inhibitory effects of the compounds isolated from W. trichotoma on β-hexosaminidase release by IgE + DNP-BSA-induced RBL-2H3 cells. Data are presented as means ± SDs (n = 2), and significant was accepted for ### p values < 0.001 versus non-treated cells, and * p < 0.05, ** p < 0.01, *** p < 0.001 versus IgE + DNP-BSA-treated cells. IgE, immunoglobulin E; DNP-BSA, 2,4-dinitrophenylated-bovine serum albumin; CsA, cyclosporin A.

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